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Joy

People share unforgettable stories told by their grandparents, and some are just insane

These grandparents truly lived.

stories from grandparents reddit

When your grandpa's a BAMF.

It can be eye-opening to listen to stories told by our grandparents. For many of us, that might be the only connection we have to them.

Even the smallest glimpse into their former lives gives us insight–not only into their own personal history, but into the soul of a different era entirely. Of course, whether that inspires nostalgia or disgust depends on the story.

I, for instance, know next-to-nothing about my maternal grandfather, other than he used his job at a candy factory to cover the fact that he was in cahoots with an Asian mob. An odd thing to know about your grandfather, and I’ll never look at M&M’s the same way again.

stories from grandparentsGiphy

A Reddit user named LorieEve recently asked people to share stories from their own grandparents that they’d “never forget.” Some answers are short and simple. Others read like a sprawling novel. Some are hilarious; others heartbreaking. All offer a meaningful look into the past.

Here are 10 of the best responses:


1.

My grandfather was one of the earliest people to receive penicillin. His GP freaked out when he had a handwritten note from Alexander Fleming.” – melodicmusical

2.

"My grandpa worked in a steel mill in Ohio during the 50s and 60s and he was robbed at gunpoint in the basement of said mill when he looked him in the eyes and said ‘nice gun, but mine’s bigger’ needless to say he was not robbed.

He was also launched out of a third story window and landed in a dumpster from a propane explosion. He had suffered 3rd degree burns and drove the other 3 people involved to the hospital where they received proper care. His scars are covered by his beard.

He was also involved in a helicopter crash that destroyed his back so he can no longer sit down very well. He also survived an airplane crash in the 50s when 3 out of the 4 engines lost power and caught fire. It was a military aircraft that had been repurposed after the war.

In the 60s he was involved in a car accident caused by 2 people who had just robbed a bank. He then helped the police chase them down in his partially destroyed car because he wanted insurance information.

There was also the time that his senile grandfather shot him in his back with a shotgun but luckily he was far enough away that the pellets didn't penetrate very far.

In short, some of his stories may be made up, or my he's literally John Wick.” – that_one_nerd470

3.

My grandmother's brother was drafted in the Army and was sent to fight in the Korean War. He ended up in the 2nd Infantry Division. His division was caught in The Gauntlet and he didn’t make it back home. To this day, he is still unaccounted for.

Well, the day he left home the last time, my grandma went with him to the train station. She told me that the last thing he ever said to her was, ‘at least I made it back home for a home cooked meal before I left.’

She was probably well into her 70s when she told me that story. It still brought tears to her eyes.” – slider728

4.

My grandparents and all my relatives of that generation fled Germany after my great-grandfather was taken to a work camp.

My grandmother's most haunting story:

She was about 14, walking with a boy in their town square. She had blonde hair and would definitely 'pass' for Aryan. He apparently fit what the SS thought of as a Jew (he may have been wearing a yarmulke or other garment, I never knew that part.) The officers stopped them and grabbed him, told him to stay away from Aryan girls. He tried to say something, but didn't get to before they handcuffed him and dragged him away. They wished my grandmother goodnight and she never saw him again.” – DTownForever

5.

My grandmother's family fled for their lives from Austria to the USA. Her father had been an outspoken political opponent of Adolf Hitler, and helped organize an anti-Nazi resistance in his hometown. Then Hitler invaded Austria, and somebody was kind enough to tip my great-grandpa off that his name was on a list to get shipped off to the concentration camps.

My grandmother barely remembered Austria or the move to New York City. But she never forgot a year or so later walking into a store with her father one day, only to have the shopkeeper curse him out and refuse to serve him as soon as he opened his mouth and spoke with a German accent. That incident made a deep impression on her. She credited it with teaching her quickly…just how shitty prejudice can be, especially in times of war.

She never taught any of her children her native language. An enormous number of German-Americans lost or refused to pass on their heritage language during WWII, because that wasn't a great time to be visibly German in any way in the USA.” – hononononnoh

6.

My grandfather was a kid during the Great Depression. He once told me they had raccoon one year for a special Christmas dinner.” – FlokiTrainer

7.

This one's more lighthearted than most.

Both of my grandparents grew up in South Africa, and dated throughout high school. Just as they're getting ready to graduate, Ouma's father decided to move the whole family to the US. Totally heartbroken, Ouma broke up with Oupa a week before the departure, then spent the next few days bawling her eyes out in between packing. To her surprise Oupa had 'taken the news way too well'.

On the day of the departure Ouma and her family arrive to find Oupa waiting on the dock for them. Ouma figured he was there to see them off, until she realizes that the suitcases all around his feet are his. And when he went to greet them he was holding a letter from his parents for her parents, a ticket for their ship, and an engagement ring. Turns out that man had looked so calm during the breakup because he'd already been planning on going across the ocean for her.

They're up in their eighties and still together now.” – Anxious_Cap51

8.

When my grandpa was 9 ish him and his friends were playing by the train tracks as people in their generation did. Him and his friends convinced a 4 year old who was playing with them at the time to get on a random train carriage where they then closed the door and told him he was going to Blackpool, he tried to frantically unlock the door but was too small to reach the lock.

He recalls watching this little boy's face as the train pulled off from the station.

After an hour the boy's mother asked them all where her son was where they just said ‘oh he's off to Blackpool.’ Luckily at the next train station a train conductor found the little boy and took him back on the next train.” – Remarkable-Ad-1107

9.

My grandfather was quite the badass when he was younger, lots of stories I remember from him, but I’ve gotta share this story:

Context, I’m a second gen Canadian which makes my grandparents the ones who immigrated. They immigrated from the Netherlands, which is popular for their culture, food, and of course beer.

When he immigrated to Canada, he knew some English but not much...There was a man who greeted my grandfather which I don’t remember how or when, but regardless, they got to talking and the man asked my grandfather to ‘go for a beer’. And in Holland when you're asked to go for a beer, it means go to the bar and go get a beer.

Note this was the late 60’s in Canada, and A&W was beginning to be popular. My grandfather of course agrees, to get to know more people around where he was going to live. The man brings my grandfather to A&W, for a root beer and a burger, so he was confused out of his mind not being able to speak a word of English in this new country, and trying to learn the culture. My grandfather then learned he hated root beer. He still has contact with the A&W man.” – I-am-johan

10.

My grandfather was a veteran of WWII, and one of the toughest but kindest people I ever had the honor of knowing.

One story from his military service he enjoyed sharing was his issues with driving on base. He was pulling up to his DI’s office, and went for a soft brake and park. Instead, due to how close the brake and gas pedals were in the truck he was driving, he hit the gas, and crashed into his DI’s office, stopping right at his desk.

While his DI stood there in shock and likely anger, my grandfather got out of the truck and just said hi. To which his DI responded ‘Hi? HI?! WHAT IS THE MATTER WITH YOU?!’

I miss my grandfather every day, and if there is a heaven, I hope he’s staying away from those trucks.” – SuburbanDJ

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

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It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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